US6093686A - Liquid for contact lenses - Google Patents
Liquid for contact lenses Download PDFInfo
- Publication number
- US6093686A US6093686A US09/265,544 US26554499A US6093686A US 6093686 A US6093686 A US 6093686A US 26554499 A US26554499 A US 26554499A US 6093686 A US6093686 A US 6093686A
- Authority
- US
- United States
- Prior art keywords
- liquid
- contact lenses
- polymer
- contact lens
- contact
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 84
- 230000002421 anti-septic effect Effects 0.000 claims abstract description 39
- 229920000642 polymer Polymers 0.000 claims abstract description 30
- 238000004321 preservation Methods 0.000 claims abstract description 21
- 239000004094 surface-active agent Substances 0.000 claims description 29
- 238000004140 cleaning Methods 0.000 claims description 23
- 239000002738 chelating agent Substances 0.000 claims description 13
- 230000000249 desinfective effect Effects 0.000 claims description 12
- 229920000083 poly(allylamine) Polymers 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 239000002562 thickening agent Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 238000004659 sterilization and disinfection Methods 0.000 claims description 3
- 101150108015 STR6 gene Proteins 0.000 claims 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 10
- 239000002202 Polyethylene glycol Substances 0.000 description 16
- 229920001223 polyethylene glycol Polymers 0.000 description 16
- 230000000694 effects Effects 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- -1 polyoxyethylene Polymers 0.000 description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- 229910052708 sodium Inorganic materials 0.000 description 12
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 11
- 229910052760 oxygen Inorganic materials 0.000 description 11
- 239000001301 oxygen Substances 0.000 description 11
- 241000894006 Bacteria Species 0.000 description 10
- 125000000129 anionic group Chemical group 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 238000012423 maintenance Methods 0.000 description 5
- 230000003204 osmotic effect Effects 0.000 description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 3
- 229940064004 antiseptic throat preparations Drugs 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229960000502 poloxamer Drugs 0.000 description 3
- 229920001983 poloxamer Polymers 0.000 description 3
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920002413 Polyhexanide Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- OSASVXMJTNOKOY-UHFFFAOYSA-N chlorobutanol Chemical compound CC(C)(O)C(Cl)(Cl)Cl OSASVXMJTNOKOY-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- QTKPMCIBUROOGY-UHFFFAOYSA-N 2,2,2-trifluoroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)F QTKPMCIBUROOGY-UHFFFAOYSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 206010016275 Fear Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229960003260 chlorhexidine Drugs 0.000 description 1
- 229960004926 chlorobutanol Drugs 0.000 description 1
- KXKPYJOVDUMHGS-OSRGNVMNSA-N chondroitin sulfate Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](OS(O)(=O)=O)[C@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(O)=O)O1 KXKPYJOVDUMHGS-OSRGNVMNSA-N 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- WPUMTJGUQUYPIV-JIZZDEOASA-L disodium (S)-malate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](O)CC([O-])=O WPUMTJGUQUYPIV-JIZZDEOASA-L 0.000 description 1
- WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- QFRWWTBTWUSSDA-UHFFFAOYSA-M mercury(1+);2-phenylacetate Chemical compound [Hg+].[O-]C(=O)CC1=CC=CC=C1 QFRWWTBTWUSSDA-UHFFFAOYSA-M 0.000 description 1
- OAGNPTDOULFGJY-UHFFFAOYSA-N mercury;phenyl nitrate Chemical compound [Hg].[O-][N+](=O)OC1=CC=CC=C1 OAGNPTDOULFGJY-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 125000005401 siloxanyl group Chemical group 0.000 description 1
- 235000019265 sodium DL-malate Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 239000001394 sodium malate Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0078—Compositions for cleaning contact lenses, spectacles or lenses
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
Definitions
- the present invention relates to a liquid for contact lenses. More particularly, the present invention relates to a liquid for contact lenses which can be preferably used for preservation, cleaning and disinfection of contact lenses.
- contact lenses in particular oxygen permeable hard contact lenses, are prepared by using a silicone component. Accordingly, the lens surface becomes hydrophobic and wettability of the lens at initial wearing is poor. As a result, wearing sensation is lowered and sight cannot be sufficiently recovered.
- the above oxygen permeable hard contact lens is subjected to surface treatment or immersed in a preserving solution such as physiological sodium chloride solution.
- bacteria may propagate in a preserving solution during preservation of a contact lens. Accordingly, in order to prevent bacteria from propagating, an antiseptic is added to the preserving solution.
- the antiseptic effect of the antiseptic is sometimes insufficient, or some of the antiseptics are poor in safety and durability. Accordingly, such antiseptics are not effective for preventing the propagation of bacteria.
- the antiseptic in the case when a soft contact lens is immersed in the above preserving solution containing an antiseptic, the antiseptic sometimes adheres to the surface of the soft contact lens or is sometimes captured in the inside of the lens. Accordingly, it is desired that there is developed a method comprising using a polymerized antiseptic.
- An object of the present invention is to provide a liquid for contact lenses, which can substantially decrease the variation of the base curve of a contact lens, in particular an oxygen permeable hard contact lens during preservation, and which shows an excellent antiseptic effect, an excellent antibacterial effect and durability of these effects.
- a liquid for contact lenses containing a polymer (A) having a recurring unit represented by the formula (I): ##STR2## wherein n is 0 or 1.
- the liquid for contact lenses of the present invention is excellent in solubility and appearance, has a not unpleasant smell, and shows stability of antiseptic effect and antibacterial effect for a long period of time. Therefore, when a contact lens, in particular, an oxygen permeable hard contact lens is preserved in the liquid for contact lenses of the present invention, variation of the base curve which is one of important standards of a contact lens can be considerably decreased.
- the liquid for contact lenses of the present invention contains a polymer (A) having a recurring unit represented by the formula (I): ##STR3## wherein n is 0 or 1.
- the above polymer (A) is an effective ingredient for decreasing the variation of base curve of a contact lens during preservation and further imparting an antiseptic effect and an antibacterial effect.
- a polyallylamine having a recurring unit represented by the formula: ##STR4## is preferably used.
- the polymer (A) In order to sufficiently provide stability of the base curve of a contact lens and sufficiently provide an antiseptic effect and antibacterial an effect, the polymer (A) needs to have a certain molecular weight. Accordingly, it is desired that weight average molecular weight of the polymer (A) is at least about 500, preferably at least about 1000. In order to remove fears that solubility of the polymer (A) in a medium such as water is reduced so that a uniform liquid for contact lenses cannot be easily prepared, and that handling of the polymer (A) is reduced due to increase of viscosity, it is desired that weight average molecular weight of the polymer (A) is at most about 200000, preferably at most about 100000.
- Various polymers (A) can be used alone or in admixture thereof.
- the content of the polymer (A) in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.1 w/v %.
- the content of the polymer (A) in the liquid for contact lenses is at most 10 w/v %, preferably at most 3 w/v %.
- the liquid for contact lenses can contain, for instance, an antiseptic, a chelating agent and the like in addition to the above polymer (A).
- the above antiseptic is a component for preventing contamination for the liquid for contact lenses with germs and preventing contamination for a contact lens with bacteria during preservation in the liquid for contact lenses.
- the antiseptic effect and antibacterial effect which are exhibited from the polymer (A) can be further increased.
- the antiseptic is an ophthalmic physiologically acceptable component and is not particularly limited.
- Typical examples of the added antiseptic are, for instance, a mercury antiseptic such as mercury phenyl nitrate, mercury phenyl acetate or thimerosal; a surface active agent type antiseptic such as benzalkonium chloride or pyridinium bromide; an alcohol antiseptic such as chlorhexidine, polyhexamethylene biguanide or chlorobutanol; methylparaben, propylparaben, dimethyloldimethylhydantoin, imidazoliumurea; and the like. These can be used alone or in admixture thereof.
- the content of the added antiseptic in the liquid for contact lenses is at least 0.00001 w/v %, preferably at least 0.00003 w/v %.
- the content of the added antiseptic in the liquid for contact lenses is at most 0.5 w/v %, preferably at most 0.3 w/v %.
- the above noted added chelating agent is a component for preventing calcium, which is included in the liquid for contact lenses or lacrimal fluid adhering a contact lens, from accumulating on a contact lens.
- the chelating agent is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the chelating agent are, for instance, ethylenediaminetetraacetic acid, sodium ethylenediaminetetraacetate, phytic acid, citric acid and the like. These can be used alone or in admixture thereof.
- the content of the chelating agent in the liquid for contact lenses is at least 0.001 mol/l, preferably at least 0.0015 mol/l.
- the content of the chelating agent in the liquid for contact lenses is at most 0.1 mol/l, preferably at most 0.05 mol/l.
- the liquid for contact lenses can contain, for instance, other additives such as a buffer, an isotonizing agent, a thickener and a surface active agent in addition to the antiseptic and the chelating agent.
- other additives such as a buffer, an isotonizing agent, a thickener and a surface active agent in addition to the antiseptic and the chelating agent.
- the above buffer is a component for setting pH of the liquid for contact lenses within the range of about 5 to 9 near to pH of lacrimal fluid, preventing variation of the pH of the liquid for contact lenses, due to any outside influence, and protecting shape and optical property of a contact lens during preservation.
- the buffer is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the buffer are, for instance, boric acid, sodium borate, phosphoric acid, sodium phosphate, citric acid, sodium citrate, lactic acid, sodium lactate, glycine, an amino acid such as glutamic acid, sodium salt of an amino acid, malic acid, sodium malate and the like. These can be used alone or in admixture thereof.
- the content of the buffer in the liquid for contact lenses is at least 0.005 mol/l, preferably at least 0.01 mol/l.
- the content of the buffer in the liquid for contact lenses is too large, there is a tendency that buffer effect is not very much additionally improved and osmotic pressure is heightened, so an adverse influence is imparted to shape of a contact lens. Accordingly, it is desired that the content of the buffer in the liquid for contact lenses is at most 0.5 mol/l, preferably at most 0.15 mol/l.
- the above isotonizing agent is a component for setting osmotic pressure of the liquid for contact lenses within the range of 280 to 320 mOs/kg near to osmotic pressure of lacrimal fluid, and supporting maintenance of shape of a contact lens during preservation.
- the isotonizing agent is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the isotonizing agent are, for instance, an inorganic salt such as sodium chloride, potassium chloride or calcium chloride; compounds which are exemplified as the above buffer; and the like. These can be used alone or in admixture thereof.
- the content of the isotonizing agent in the liquid for contact lenses is at least 0.01 mol/l, preferably at least 0.05 mol/l.
- the content of the isotonizing agent in the liquid for contact lenses is at most 0.5 mol/l, preferably at most 0.15 mol/l.
- the above noted is a component for protecting a contact lens from outside stress during preservation.
- the thickener is an ophthalmic physiologically acceptable component and is not particularly limited.
- Typical examples of the thickener are, for instance, a viscous substance such as polyvinyl alcohol, poly-N-vinylpyrrolidone, polyacrylamide, hydrolyzate of polyacrylamide, polyacrylic acid, xanthane gum, hydroxyethylcellulose, carboxymethylcellulose, methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcellulose, sodium alginate, polyethylene glycol, gelatin, sodium chondroitin sulfate or gum arabic; and the like. These can be used alone or in admixture thereof.
- the content of the thickener in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %.
- the content of the thickener in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
- the above surface active agent is a component for further improving the cleaning effect of the liquid for contact lenses.
- the surface active agent is an ophthalmic physiologically acceptable component and is not particularly limited.
- Various surface active agents such as an anionic surface active agent, a nonionic surface active agent and a combination of anionic surface active agent with nonionic surface active agent can be used.
- anionic surface active agent examples include, for instance, sodium alkylsulfate sodium alkylbenzenesulfonate, sodium alkyloylmethyltaurinate, sodium alkyloylsarcosinate, sodium ⁇ -olefinsulfonate, sodium polyoxyethylene alkyl ether phosphate, sodium polyoxyethylene alkyl ether sulfate, sodium polyoxyethylene alkyl phenyl ether sulfate, sodium di(polyoxyethylene alkyl ether) phosphate and the like. These can be used alone or in admixture thereof.
- sodium alkylsulfate, sodium alkylbenzenesulfonate, sodium ⁇ -olefinsulfonate, sodium polyoxyethylene alkyl ether sulfate and sodium polyoxyethylene alkyl phenyl ether sulfate show excellent cleaning effect, and are preferable.
- anionic surface active agents are used with the nonionic surface active agent, effective cleaning effect is exhibited during immersion and preservation for a short period of time.
- the content of the anionic surface active agent in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %.
- the content of the anionic surface active agent in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
- nonionic surface active agent are, for instance, an adduct of higher alkylamine with polyethylene glycol, an adduct of higher fattyamide with polyethylene glycol, an ester of polyglycerin with higher fatty acid, an ester of a polyalkylene glycol such as polyethylene glycol with higher fatty acid, a polyethylene glycol copolymer ester, an ester of adduct (of polyvalent alcohol with polyethylene glycol) with higher fatty acid, an ether of polyethylene glycol with higher alcohol, an ether of polyglycerin with higher alcohol, an ether of polyethylene glycol with alkylphenol, a condensate of ether (of polyethylene glycol with alkylenephenol) with formaldehyde, a polypropylene glycol-polyethylene glycol copolymer, a phosphate, castor oil, hydrogenated castor oil, a sorbitan alkylester of polyethylene glycol, an adduct of sterol with poly
- an ether of polyethylene glycol with higher alcohol an ester of polyethylene glycol with higher fatty acid, an ester of polyglycerin with higher fatty acid, an ether of polyethylene glycol with alkylphenol, a sorbitan alkylester of polyethylene glycol and poloxamer show excellent cleaning effect, and are preferable.
- the content of the nonionic surface active agent in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %.
- the content of the nonionic surface active agent in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
- the anionic surface active agent and the nonionic surface active agent are used at the same time, it is desired that the content of the anionic surface active agent and the content of the nonionic surface active agent are within the above defined range, respectively. Also, it is desired that the total amount of the anionic surface active agent and the nonionic surface active agent in the liquid for contact lenses is 0.02 to 20 w/v %, preferably 0.05 to 10 w/v %.
- the liquid for contact lenses of the present invention contains the polymer (A) as an effective ingredient and, as occasion demands, contains the antiseptic, the chelating agent and the other additives.
- a medium water such as distilled water or purified water may be contained in the liquid for contact lenses. The amount of an aqueous medium such as water is adjusted so that the total amount of the liquid for contact lenses reaches 100%.
- the polymer (A) is added to the prescribed amount of the aqueous medium and, as occasion demands, the additives such as antiseptic, chelating agent, buffer, isotonizing agent, thickener and surface active agent are added thereto. These are sufficiently mixed and stirred with each other, and the polymer (A) and the additives are dissolved in the aqueous medium to give a solution. Then, the solution is filtrated to give the liquid for contact lenses of the present invention.
- the additives such as antiseptic, chelating agent, buffer, isotonizing agent, thickener and surface active agent are added thereto.
- Viscosity of the liquid for contact lenses is not particularly limited. In consideration of handling during preservation of a contact lens, it is preferable that viscosity of the liquid for contact lenses is at most about 200 cP at 25° C.
- pH of the liquid for contact lenses is 5 to 9, which is much the same as pH of lacrimal fluid.
- the various contact lenses can be preserved with hardly varying the base curve thereof.
- contamination for the liquid for contact lenses itself with bacteria can be prevented and various contact lenses can be cleaned or disinfected in the liquid for contact lenses.
- the liquid for contact lenses of the present invention can be suitably used as a preserving solution, a cleaning solution, a disinfecting solution or a liquid used for at least two of preservation, cleaning and disinfection.
- a contact lens can be preserved, cleaned or disinfected by entirely immersing itself in the liquid for contact lenses in the prescribed vessel and sealing up the vessel.
- a contact lens which is preserved, cleaned or disinfected in the liquid for contact lenses is not particularly limited.
- Various contact lenses such as a water-absorptive contact lens and a non-water-absorptive contact lens can be applied.
- various contact lenses such as a soft contact lens and a hard contact lens can be applied.
- an oxygen permeable hard contact lens prepared by polymerizing a monomer mixture containing silicone compounds such as a siloxanyl (meth)acrylate monomer, a siloxanylstyrene monomer, a siloxanyl fumarate and a siloxanyl itaconate is immersed in the liquid for contact lenses, variation of base curve of the oxygen permeable hard contact lens can be considerably decreased during preservation.
- Polyallylamine having a weight average molecular weight of about 10000 and a recurring unit represented by the formula: ##STR5## (hereinafter referred to as polyallylamine (1)) was added to distilled water. They were stirred at room temperature or with slightly heating for about 60 minutes to dissolve polyallylamine (1) in the distilled water. The obtained solution was filtrated to give 300 ml of a preserving solution for contact lenses, containing 0.5 w/v % of polyallylamine (1).
- Appearance of the preserving solution for contact lenses was observed with naked eyes and evaluated according to the following criteria for evaluation.
- the preserving solution is uniform and transparent.
- viscosity (cP) of the preserving solution for contact lenses was measured at 25° C.
- a monomer mixture of 50 parts by weight of siloxanyl methacrylate, 40 parts by weight of trifluoroethyl methacrylate, 10 parts by weight of methyl methacrylate and 5 parts by weight of ethylene glycol dimethacrylate was copolymerized to give a polymer.
- the polymer was molded to give an oxygen permeable hard contact lens having a thickness of 0.12 mm.
- the five oxygen permeable hard contact lenses and the preserving solution for contact lenses were put in a case for contact lenses.
- the five oxygen permeable hard contact lenses were immersed in the preserving solution for contact lenses, and the case was sealed up and maintained at 40° C. After 2 weeks and 4 weeks, each base curve of the five oxygen permeable hard contact lenses was measured.
- the variation coefficient of base curve was calculated in the same manner as in Example 1 except that physiological sodium chloride solution was used instead of the preserving solution for contact lenses in Example 1. The results are shown in Table 1.
- Example 2 In the same manner as in Example 1 except that 0.5 ppm (weight) of polyhexamethylene biguanide and 1 w/v % (0.033 mol/l) of ethylenediaminetetraacetic acid were added to distilled water together with 0.5 w/v % of polyallylamine (1) in Example 1, 300 ml of a cleaning and disinfecting solution for contact lenses was prepared.
- Example 1 Using the cleaning and disinfecting solution for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
- Example 2 In the same manner as in Example 1 except that 0.1 w/v % of poloxamer and 0.1 w/v % (0.0033 mol/l) of ethylenediaminetetraacetic acid were added to distilled water together with 0.5 w/v % of polyallylamine (1) in Example 1, and further isotonization was carried out using 1 mol/l of sodium chloride, 300 ml of a cleaning and disinfecting solution for contact lenses was prepared.
- Example 1 Using the cleaning and disinfecting solution for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
- Example 1 Using the obtained liquid for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
- the preserving solution for contact lenses were inoculated 1.0 ⁇ 10 6 Gram-positive vegetative bacteria (Staphylococcus aureus) and 1.0 ⁇ 10 6 Gram-negative vegetative bacteria (Escherichia coli). Then, the preserving solution for contact lenses was allowed to stand at 37° C. for 24 hours. After 24 hours, the number of each bacteria in the preserving solution for contact lenses was measured.
- the preserving solution for contact lenses shows excellent antiseptic effect and excellent antibacterial effect.
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Abstract
A liquid for contact lenses, containing a polymer (A) having a recurring unit represented by the formula (I): wherein n is 0 or 1. The liquid for contact lenses can considerably decrease variation of the base curve of a contact lens during preservation, and shows excellent antiseptic effect and excellent antibacterial effect.
Description
The present invention relates to a liquid for contact lenses. More particularly, the present invention relates to a liquid for contact lenses which can be preferably used for preservation, cleaning and disinfection of contact lenses.
In general, most of contact lenses, in particular oxygen permeable hard contact lenses, are prepared by using a silicone component. Accordingly, the lens surface becomes hydrophobic and wettability of the lens at initial wearing is poor. As a result, wearing sensation is lowered and sight cannot be sufficiently recovered.
Therefore, in order to maintain surface wettability during preservation when not being worn, the above oxygen permeable hard contact lens is subjected to surface treatment or immersed in a preserving solution such as physiological sodium chloride solution.
However, in the case that a contact lens is preserved in such physiological sodium chloride solution, the base curve which is one of the important standards of a contact lens sometimes varies.
For instance, bacteria may propagate in a preserving solution during preservation of a contact lens. Accordingly, in order to prevent bacteria from propagating, an antiseptic is added to the preserving solution.
However, the antiseptic effect of the antiseptic is sometimes insufficient, or some of the antiseptics are poor in safety and durability. Accordingly, such antiseptics are not effective for preventing the propagation of bacteria.
In particular, in the case when a soft contact lens is immersed in the above preserving solution containing an antiseptic, the antiseptic sometimes adheres to the surface of the soft contact lens or is sometimes captured in the inside of the lens. Accordingly, it is desired that there is developed a method comprising using a polymerized antiseptic.
An object of the present invention is to provide a liquid for contact lenses, which can substantially decrease the variation of the base curve of a contact lens, in particular an oxygen permeable hard contact lens during preservation, and which shows an excellent antiseptic effect, an excellent antibacterial effect and durability of these effects.
This and other objects of the present invention will become apparent from the description hereinafter.
In accordance with the present invention, there is provided a liquid for contact lenses, containing a polymer (A) having a recurring unit represented by the formula (I): ##STR2## wherein n is 0 or 1.
The liquid for contact lenses of the present invention is excellent in solubility and appearance, has a not unpleasant smell, and shows stability of antiseptic effect and antibacterial effect for a long period of time. Therefore, when a contact lens, in particular, an oxygen permeable hard contact lens is preserved in the liquid for contact lenses of the present invention, variation of the base curve which is one of important standards of a contact lens can be considerably decreased.
The liquid for contact lenses of the present invention contains a polymer (A) having a recurring unit represented by the formula (I): ##STR3## wherein n is 0 or 1.
In the liquid for contact lenses, the above polymer (A) is an effective ingredient for decreasing the variation of base curve of a contact lens during preservation and further imparting an antiseptic effect and an antibacterial effect.
In the present invention, because the variation of the base curve of a contact lens can be considerably decreased and the antiseptic effect and antibacterial the effect can be greatly exhibited, a polyallylamine having a recurring unit represented by the formula: ##STR4## is preferably used.
In order to sufficiently provide stability of the base curve of a contact lens and sufficiently provide an antiseptic effect and antibacterial an effect, the polymer (A) needs to have a certain molecular weight. Accordingly, it is desired that weight average molecular weight of the polymer (A) is at least about 500, preferably at least about 1000. In order to remove fears that solubility of the polymer (A) in a medium such as water is reduced so that a uniform liquid for contact lenses cannot be easily prepared, and that handling of the polymer (A) is reduced due to increase of viscosity, it is desired that weight average molecular weight of the polymer (A) is at most about 200000, preferably at most about 100000.
Various polymers (A) can be used alone or in admixture thereof.
In order to sufficiently decrease variation of base curve of a contact lens during preservation and further sufficiently provide both an antiseptic effect and an antibacterial effect, it is desired that the content of the polymer (A) in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.1 w/v %. In order to remove a fear that a contact lens is easily stained when dried and handling is lowered because viscosity of the liquid for contact lenses is too great, it is desired that the content of the polymer (A) in the liquid for contact lenses is at most 10 w/v %, preferably at most 3 w/v %.
The liquid for contact lenses can contain, for instance, an antiseptic, a chelating agent and the like in addition to the above polymer (A).
The above antiseptic is a component for preventing contamination for the liquid for contact lenses with germs and preventing contamination for a contact lens with bacteria during preservation in the liquid for contact lenses. By using the added antiseptic, the antiseptic effect and antibacterial effect which are exhibited from the polymer (A) can be further increased.
The antiseptic is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the added antiseptic are, for instance, a mercury antiseptic such as mercury phenyl nitrate, mercury phenyl acetate or thimerosal; a surface active agent type antiseptic such as benzalkonium chloride or pyridinium bromide; an alcohol antiseptic such as chlorhexidine, polyhexamethylene biguanide or chlorobutanol; methylparaben, propylparaben, dimethyloldimethylhydantoin, imidazoliumurea; and the like. These can be used alone or in admixture thereof.
In order to sufficiently exhibit further antiseptic effect, it is desired that the content of the added antiseptic in the liquid for contact lenses is at least 0.00001 w/v %, preferably at least 0.00003 w/v %. When the content of the added antiseptic in the liquid for contact lenses is too large, there are adverse tendencies that the antiseptic directly inserts into that eyes, so that eyes are injured, and that some of the antiseptics impart adverse influence to standards and properties of a contact lens. Accordingly, it is desired that the content of the added antiseptic in the liquid for contact lenses is at most 0.5 w/v %, preferably at most 0.3 w/v %.
The above noted added chelating agent is a component for preventing calcium, which is included in the liquid for contact lenses or lacrimal fluid adhering a contact lens, from accumulating on a contact lens.
The chelating agent is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the chelating agent are, for instance, ethylenediaminetetraacetic acid, sodium ethylenediaminetetraacetate, phytic acid, citric acid and the like. These can be used alone or in admixture thereof.
In order to sufficiently exhibit effect of preventing accumulation of calcium on a contact lens, it is desired that the content of the chelating agent in the liquid for contact lenses is at least 0.001 mol/l, preferably at least 0.0015 mol/l. When the content of the chelating agent in the liquid for contact lenses is too large, there is a tendency that effects are not very much improved considering the content, so economy is lowered. Accordingly, it is desired that the content of the chelating agent in the liquid for contact lenses is at most 0.1 mol/l, preferably at most 0.05 mol/l.
The liquid for contact lenses can contain, for instance, other additives such as a buffer, an isotonizing agent, a thickener and a surface active agent in addition to the antiseptic and the chelating agent.
The above buffer is a component for setting pH of the liquid for contact lenses within the range of about 5 to 9 near to pH of lacrimal fluid, preventing variation of the pH of the liquid for contact lenses, due to any outside influence, and protecting shape and optical property of a contact lens during preservation.
The buffer is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the buffer are, for instance, boric acid, sodium borate, phosphoric acid, sodium phosphate, citric acid, sodium citrate, lactic acid, sodium lactate, glycine, an amino acid such as glutamic acid, sodium salt of an amino acid, malic acid, sodium malate and the like. These can be used alone or in admixture thereof.
In order to sufficiently exhibit buffer effect, it is desired that the content of the buffer in the liquid for contact lenses is at least 0.005 mol/l, preferably at least 0.01 mol/l. When the content of the buffer in the liquid for contact lenses is too large, there is a tendency that buffer effect is not very much additionally improved and osmotic pressure is heightened, so an adverse influence is imparted to shape of a contact lens. Accordingly, it is desired that the content of the buffer in the liquid for contact lenses is at most 0.5 mol/l, preferably at most 0.15 mol/l.
The above isotonizing agent is a component for setting osmotic pressure of the liquid for contact lenses within the range of 280 to 320 mOs/kg near to osmotic pressure of lacrimal fluid, and supporting maintenance of shape of a contact lens during preservation.
The isotonizing agent is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the isotonizing agent are, for instance, an inorganic salt such as sodium chloride, potassium chloride or calcium chloride; compounds which are exemplified as the above buffer; and the like. These can be used alone or in admixture thereof.
In order to sufficiently impart osmotic pressure to the liquid for contact lenses, it is desired that the content of the isotonizing agent in the liquid for contact lenses is at least 0.01 mol/l, preferably at least 0.05 mol/l. When the content of the isotonizing agent in the liquid for contact lenses is too large, there is a tendency that osmotic pressure is heightened, so an adverse influence is imparted to shape of a contact lens. Accordingly, it is desired that the content of the isotonizing agent in the liquid for contact lenses is at most 0.5 mol/l, preferably at most 0.15 mol/l.
The above noted is a component for protecting a contact lens from outside stress during preservation.
The thickener is an ophthalmic physiologically acceptable component and is not particularly limited. Typical examples of the thickener are, for instance, a viscous substance such as polyvinyl alcohol, poly-N-vinylpyrrolidone, polyacrylamide, hydrolyzate of polyacrylamide, polyacrylic acid, xanthane gum, hydroxyethylcellulose, carboxymethylcellulose, methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcellulose, sodium alginate, polyethylene glycol, gelatin, sodium chondroitin sulfate or gum arabic; and the like. These can be used alone or in admixture thereof.
In order to sufficiently protect a contact lens from outside stress during preservation, it is desired that the content of the thickener in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %. When the content of the thickener in the liquid for contact lenses is too large, there is a tendency that the liquid for contact lenses becomes gelated, so the preservative property is lowered. Accordingly, it is desired that the content of the thickener in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
The above surface active agent is a component for further improving the cleaning effect of the liquid for contact lenses.
The surface active agent is an ophthalmic physiologically acceptable component and is not particularly limited. Various surface active agents such as an anionic surface active agent, a nonionic surface active agent and a combination of anionic surface active agent with nonionic surface active agent can be used.
Typical examples of the anionic surface active agent are, for instance, sodium alkylsulfate sodium alkylbenzenesulfonate, sodium alkyloylmethyltaurinate, sodium alkyloylsarcosinate, sodium α-olefinsulfonate, sodium polyoxyethylene alkyl ether phosphate, sodium polyoxyethylene alkyl ether sulfate, sodium polyoxyethylene alkyl phenyl ether sulfate, sodium di(polyoxyethylene alkyl ether) phosphate and the like. These can be used alone or in admixture thereof. Among them, sodium alkylsulfate, sodium alkylbenzenesulfonate, sodium α-olefinsulfonate, sodium polyoxyethylene alkyl ether sulfate and sodium polyoxyethylene alkyl phenyl ether sulfate show excellent cleaning effect, and are preferable. When these anionic surface active agents are used with the nonionic surface active agent, effective cleaning effect is exhibited during immersion and preservation for a short period of time.
In order to sufficiently exhibit cleaning effect, it is desired that the content of the anionic surface active agent in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %. When the content of the anionic surface active agent in the liquid for contact lenses is too large, there is a tendency that cleaning effect is not very much further improved and hands become rough. Accordingly, it is desired that the content of the anionic surface active agent in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
Typical examples of the nonionic surface active agent are, for instance, an adduct of higher alkylamine with polyethylene glycol, an adduct of higher fattyamide with polyethylene glycol, an ester of polyglycerin with higher fatty acid, an ester of a polyalkylene glycol such as polyethylene glycol with higher fatty acid, a polyethylene glycol copolymer ester, an ester of adduct (of polyvalent alcohol with polyethylene glycol) with higher fatty acid, an ether of polyethylene glycol with higher alcohol, an ether of polyglycerin with higher alcohol, an ether of polyethylene glycol with alkylphenol, a condensate of ether (of polyethylene glycol with alkylenephenol) with formaldehyde, a polypropylene glycol-polyethylene glycol copolymer, a phosphate, castor oil, hydrogenated castor oil, a sorbitan alkylester of polyethylene glycol, an adduct of sterol with polyethylene glycol, poloxamer and the like. These can be used alone or in admixture thereof. Among them, an ether of polyethylene glycol with higher alcohol, an ester of polyethylene glycol with higher fatty acid, an ester of polyglycerin with higher fatty acid, an ether of polyethylene glycol with alkylphenol, a sorbitan alkylester of polyethylene glycol and poloxamer show excellent cleaning effect, and are preferable.
In order to sufficiently exhibit cleaning effect, it is desired that the content of the nonionic surface active agent in the liquid for contact lenses is at least 0.01 w/v %, preferably at least 0.02 w/v %. When the content of the nonionic surface active agent in the liquid for contact lenses is too large, there is a tendency that cleaning effect is not very much more improved and hands become rough. Accordingly, it is desired that the content of the nonionic surface active agent in the liquid for contact lenses is at most 10 w/v %, preferably at most 5 w/v %.
When the anionic surface active agent and the nonionic surface active agent are used at the same time, it is desired that the content of the anionic surface active agent and the content of the nonionic surface active agent are within the above defined range, respectively. Also, it is desired that the total amount of the anionic surface active agent and the nonionic surface active agent in the liquid for contact lenses is 0.02 to 20 w/v %, preferably 0.05 to 10 w/v %.
The liquid for contact lenses of the present invention contains the polymer (A) as an effective ingredient and, as occasion demands, contains the antiseptic, the chelating agent and the other additives. As a medium, water such as distilled water or purified water may be contained in the liquid for contact lenses. The amount of an aqueous medium such as water is adjusted so that the total amount of the liquid for contact lenses reaches 100%.
For instance, the polymer (A) is added to the prescribed amount of the aqueous medium and, as occasion demands, the additives such as antiseptic, chelating agent, buffer, isotonizing agent, thickener and surface active agent are added thereto. These are sufficiently mixed and stirred with each other, and the polymer (A) and the additives are dissolved in the aqueous medium to give a solution. Then, the solution is filtrated to give the liquid for contact lenses of the present invention.
Viscosity of the liquid for contact lenses is not particularly limited. In consideration of handling during preservation of a contact lens, it is preferable that viscosity of the liquid for contact lenses is at most about 200 cP at 25° C.
It is preferable that pH of the liquid for contact lenses is 5 to 9, which is much the same as pH of lacrimal fluid.
In the case that various contact lenses are immersed in the thus obtained liquid for contact lenses of the present invention, the various contact lenses can be preserved with hardly varying the base curve thereof. In addition, contamination for the liquid for contact lenses itself with bacteria can be prevented and various contact lenses can be cleaned or disinfected in the liquid for contact lenses.
The liquid for contact lenses of the present invention can be suitably used as a preserving solution, a cleaning solution, a disinfecting solution or a liquid used for at least two of preservation, cleaning and disinfection.
A contact lens can be preserved, cleaned or disinfected by entirely immersing itself in the liquid for contact lenses in the prescribed vessel and sealing up the vessel.
A contact lens which is preserved, cleaned or disinfected in the liquid for contact lenses is not particularly limited. Various contact lenses such as a water-absorptive contact lens and a non-water-absorptive contact lens can be applied. Also, various contact lenses such as a soft contact lens and a hard contact lens can be applied. Even if an oxygen permeable hard contact lens prepared by polymerizing a monomer mixture containing silicone compounds such as a siloxanyl (meth)acrylate monomer, a siloxanylstyrene monomer, a siloxanyl fumarate and a siloxanyl itaconate is immersed in the liquid for contact lenses, variation of base curve of the oxygen permeable hard contact lens can be considerably decreased during preservation.
The liquid for contact lenses of the present invention is more specifically described and explained by means of the following Examples. It is to be understood that the present invention is not limited to the Examples, and various changes and modifications may be made in the invention without departing from the spirit and scope thereof.
Polyallylamine having a weight average molecular weight of about 10000 and a recurring unit represented by the formula: ##STR5## (hereinafter referred to as polyallylamine (1)) was added to distilled water. They were stirred at room temperature or with slightly heating for about 60 minutes to dissolve polyallylamine (1) in the distilled water. The obtained solution was filtrated to give 300 ml of a preserving solution for contact lenses, containing 0.5 w/v % of polyallylamine (1).
Solubility, appearance, unpleasant or bad smell, pH and viscosity of the preserving solution for contact lenses were examined according to the following methods. The results are shown in Table 1.
Existence of insoluble components in the preserving solution for contact lenses was examined with naked eyes and evaluated according to the following criteria for evaluation.
Criteria for Evaluation
A: There are no insoluble components at all.
B: There is a slight insoluble component.
C: There are remarkably many insoluble components.
Appearance of the preserving solution for contact lenses was observed with naked eyes and evaluated according to the following criteria for evaluation.
Criteria for Evaluation
A: The preserving solution is uniform and transparent.
B: The preserving solution is slightly cloudy in white.
C: The preserving solution is remarkably cloudy in white.
Existence of bad smell of the preserving solution for contact lenses was examined at a distance of 5 cm and evaluated according to the following criteria for evaluation.
Criteria for Evaluation
A: Bad smell is not perceived at all.
B: Bad smell is slightly perceived.
C: Bad smell is remarkably perceived.
Using glass electrode type pH meter (HORIBA pH METER F-13 made by Horibaseisakusho Co., Ltd.), pH of the preserving solution for contact lenses was measured at 25° C.
Using B type viscosimeter, viscosity (cP) of the preserving solution for contact lenses was measured at 25° C.
Then, a monomer mixture of 50 parts by weight of siloxanyl methacrylate, 40 parts by weight of trifluoroethyl methacrylate, 10 parts by weight of methyl methacrylate and 5 parts by weight of ethylene glycol dimethacrylate was copolymerized to give a polymer. The polymer was molded to give an oxygen permeable hard contact lens having a thickness of 0.12 mm.
Each base curve of five pieces of the above oxygen permeable hard contact lens was previously measured. Then, the average base curve of the above five contact lenses before maintenance was calculated.
The five oxygen permeable hard contact lenses and the preserving solution for contact lenses were put in a case for contact lenses. The five oxygen permeable hard contact lenses were immersed in the preserving solution for contact lenses, and the case was sealed up and maintained at 40° C. After 2 weeks and 4 weeks, each base curve of the five oxygen permeable hard contact lenses was measured.
According to the difference between base curve of the contact lens after maintenance and previously measured base curve of the contact lens, the variation of each base curve was calculated. Then, the average variation of base curve of the five contact lenses was calculated. Using the average base curve of the five contact lenses before maintenance and the average variation of base curve of the five contact lenses, the variation coefficient of base curve (%) was calculated according to the following equation. The results are shown in Table 1.
Variation coefficient of base curve (%)={(Average variation of base curve)/(Average base curve before maintenance)}×100
The variation coefficient of base curve was calculated in the same manner as in Example 1 except that physiological sodium chloride solution was used instead of the preserving solution for contact lenses in Example 1. The results are shown in Table 1.
In the same manner as in Example 1 except that 0.5 ppm (weight) of polyhexamethylene biguanide and 1 w/v % (0.033 mol/l) of ethylenediaminetetraacetic acid were added to distilled water together with 0.5 w/v % of polyallylamine (1) in Example 1, 300 ml of a cleaning and disinfecting solution for contact lenses was prepared.
Solubility, appearance, unpleasant smell, pH and viscosity of the cleaning and disinfecting solution for contact lenses were examined in the same manner as in Example 1. The results are shown in Table 1.
Using the cleaning and disinfecting solution for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
In the same manner as in Example 1 except that 0.1 w/v % of poloxamer and 0.1 w/v % (0.0033 mol/l) of ethylenediaminetetraacetic acid were added to distilled water together with 0.5 w/v % of polyallylamine (1) in Example 1, and further isotonization was carried out using 1 mol/l of sodium chloride, 300 ml of a cleaning and disinfecting solution for contact lenses was prepared.
Solubility, appearance, bad smell, pH and viscosity of the cleaning and disinfecting solution for contact lenses were examined in the same manner as in Example 1. The results are shown in Table 1.
Using the cleaning and disinfecting solution for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
In the same manner as in Example 3 except that polyallylamine (1) was not used, 300 ml of a liquid for contact lenses was prepared.
Using the obtained liquid for contact lenses instead of the preserving solution for contact lenses in Example 1, the variation coefficient of base curve was calculated in the same manner as in Example 1. The results are shown in Table 1.
TABLE 1
______________________________________
Variation
coefficient
of base curve of
Properties of liquid for contact lenses
contact lens (%)
Solu- Appear- Bad Viscosity
After After
bility ance smell pH (cP) 2 weeks
4 weeks
______________________________________
Example
No.
1 A A A 7.2 50≧
0.1 0.2
2 A A A 7.2 50≧
0.1 0.2
3 A A A 7.2 50≧
0.1 0.2
Comparative
Example
1 -- -- -- -- -- 0.4 0.6
2 -- -- -- -- -- 0.4 0.8
______________________________________
From the results shown in Table 1, it can be understood that all liquids for contact lenses prepared in Examples 1 to 3 have suitable pH and viscosity, show excellent solubility and appearance, and give out no bad smell at all.
It can be understood that when a contact lens is preserved in the liquids for contact lenses prepared in Examples 1 to 3, the variation coefficient of the base curve of the contact lens is remarkably small, of course after preservation for 2 weeks, even after preservation for 4 weeks, compared with preservation in physiological sodium chloride solution in Comparative Example 1 and preservation in the liquid for contact lenses, not containing polyallylamine (1) in Comparative Example 2.
According to United States Pharmacopoeia, the following antiseptic effect test was carried out by the organism challenge test, and the antiseptic and antibacterial properties of the preserving solution for contact lenses prepared in Example 1 was examined.
Into the preserving solution for contact lenses were inoculated 1.0×106 Gram-positive vegetative bacteria (Staphylococcus aureus) and 1.0×106 Gram-negative vegetative bacteria (Escherichia coli). Then, the preserving solution for contact lenses was allowed to stand at 37° C. for 24 hours. After 24 hours, the number of each bacteria in the preserving solution for contact lenses was measured.
As a result, the number of Gram-positive vegetative bacteria and the number of Gram-negative vegetative bacteria were 2.0×103 and 2.4×103, respectively, and were remarkably decreased. It can be understood that the preserving solution for contact lenses shows excellent antiseptic effect and excellent antibacterial effect.
In addition to the ingredients used in the Examples, other ingredients can be used in the Examples as set forth in the specification to obtain substantially the same results.
Claims (11)
1. A liquid for replaceable and removable contact lenses containing from 0.01 to 10 w/v % of a polymer (A) having a recurring unit represented by the formula (I): ##STR6## wherein n is 0 or 1, wherein the weight average molecular weight of the polymer (A) is 500 to 200,000, said liquid functioning as a preserving solution, a cleaning solution, a disinfecting solution, or a liquid used for at least two of preservation, cleaning and disinfection.
2. The liquid for contact lenses of claim 1, wherein the polymer (A) is a polyallylamine having a recurring it represented by the formula: ##STR7##
3. The liquid for contact lenses of claim 1, which contains at least one of an antiseptic, a chelating agent, a buffer, an isotonizing agent, a thickener and a surface active agent.
4. In a combination of a removable and replaceable contact lens and a preserving liquid for preserving said contact lens and optionally having a function selected from cleaning, disinfecting and both cleaning and disinfecting said contact lens, wherein said contact lens is submerged in said liquid, the improvement wherein said liquid contains a polymer (A) having a recurring unit represented by the formula (1): wherein n is 0 or 1, and said polymer has a molecular weight of from 500 to 200,000.
5. The combination of claim 4 wherein said polymer (A) is a polyallylamine having a recurring unit represented by the formula ##STR8##
6. The combination of claim 4 wherein the content of the polymer (A) in said liquid is 0.01 to 10 w/v %.
7. The combination of claim 4 wherein said liquid contains at least one of an antiseptic, a chelating agent, a buffer, an isotonizing agent, a thickener and a surface active agent.
8. In a method of at least one of preserving a removable and replaceable contact lens, cleaning said contact lens and disinfecting said contact lens, comprising contacting said contact lens with a liquid for contact lenses to carry out at least one function selected from preserving, cleaning and disinfecting said contact lens, the improvement wherein said liquid for contact lenses contains a polymer (A) having a recurring unit represented by the formula (I): ##STR9## wherein n is 0 or 1, and wherein said polymer has a molecular weight of from 500 to 200,000.
9. The method of claim 8 wherein the polymer (A) is a polyallylamine having a recurring unit represented by the formula ##STR10## wherein n=1.
10. The method of claim 8 wherein the content of the polymer (A) in said liquid is 0.01 to 10 w/v %.
11. The method of claim 8 wherein said liquid for contact lenses further contains at least one of an antiseptic, a chelating agent, a buffer, an isotonizing agent, a thickener and a surface active agent.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP06180798A JP3936058B2 (en) | 1998-03-12 | 1998-03-12 | Contact lens solution |
| JP10-061807 | 1998-03-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US6093686A true US6093686A (en) | 2000-07-25 |
Family
ID=13181743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/265,544 Expired - Lifetime US6093686A (en) | 1998-03-12 | 1999-03-09 | Liquid for contact lenses |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US6093686A (en) |
| EP (1) | EP0942065B1 (en) |
| JP (1) | JP3936058B2 (en) |
| DE (1) | DE69917700T2 (en) |
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| WO2002058564A2 (en) | 2001-01-23 | 2002-08-01 | American Medical Systems, Inc. | Surgical articles |
| US20050288398A1 (en) * | 2001-07-20 | 2005-12-29 | Messersmith Phillip B | Polymeric compositions and related methods of use |
| US20060009550A1 (en) * | 2001-07-20 | 2006-01-12 | Messersmith Phillip B | Polymeric compositions and related methods of use |
| US20060241281A1 (en) * | 2001-07-20 | 2006-10-26 | Messersmith Phillip B | Peptidomimetic polymers for antifouling surfaces |
| US20070010595A1 (en) * | 2005-02-14 | 2007-01-11 | Mccabe Kevin P | Comfortable ophthalmic device and methods of its production |
| US20070149426A1 (en) * | 2005-11-16 | 2007-06-28 | Minick Kasey J | Lens care solutions |
| US20070208141A1 (en) * | 2006-02-16 | 2007-09-06 | Shull Kenneth R | Modified acrylic block copolymers for hydrogels and pressure sensitive wet adhesives |
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- 1999-03-11 EP EP99104875A patent/EP0942065B1/en not_active Expired - Lifetime
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Also Published As
| Publication number | Publication date |
|---|---|
| JP3936058B2 (en) | 2007-06-27 |
| JPH11258556A (en) | 1999-09-24 |
| DE69917700D1 (en) | 2004-07-08 |
| EP0942065B1 (en) | 2004-06-02 |
| EP0942065A1 (en) | 1999-09-15 |
| DE69917700T2 (en) | 2005-07-14 |
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